참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | tert-Butyl (2R)-2-methylpiperazine-1-carboxylate | HCID 10262201 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (3R)-1-[(4-chlorophenyl)sulfonyl]-3-methylpiperazine | HCID 11630465 | 78.7% |
반응 단계
To a solution of 1,1-dimethylethyl (2R)-2-methyl-1-piperazinecarboxylate (1.5 g, 07.5 mmol) in dry DCM (40 mL) was added triethylamine (2.59 mL, 18.8 mmol) and 4-chlorobenzenesulfonyl chloride (3.15 g, 10.5 mmol) and the reaction stirred at room temperature for 48 h. To the reaction was added resin supported-triamine (5 g) and the mixture stirred for 4 h. The reaction mixture was filtered and the filtrate washed with 0.5 M HCl (aq., 100 mL) followed by water (100 mL) before it was dried (MgSO4), filtered and the solvent removed in vacuo. The crude product was dissolved in DCM (40 mL) and TFA (10 mL) was added. The solution was stirred for 20 min. The solvent was evaporated and the residue tajen up in DCM (40 mL) and washed with 50% aqueous sodium bicarbonate (100 mL) followed by water (100 mL). The organic phase was dried (MgSO4), filtered and the solvent removed in vacuo to give the title compound (1.62 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08530478B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-d72421402bcd411a95caa05e81703400 |
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| 출처 메모 | uspto-grants-2013_09 |
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